HCID 23355222, compound → HCID 23355237, compound

HRID 234692Notes

Reaction equation

HRID 234692 reaction equation
Cl.Cl[CH2:3][CH2:4][NH:5][C:6]1[C:15]2[C:10](=[CH:11][C:12]([Cl:16])=[CH:13][CH:14]=2)[N:9]=[CH:8][CH:7]=1>C(#N)C>[Cl:16][C:12]1[CH:11]=[C:10]2[C:15]([C:6]([NH:5][CH2:4][CH2:3][N:9]3[CH2:8][CH2:7][CH2:6][CH2:15][CH:10]3[CH2:11][CH3:12])=[CH:7][CH:8]=[N:9]2)=[CH:14][CH:13]=1

Participants

3

Reactant 1

HCID 23355222HCID 23355222, compound

Product 1

HCID 23355237HCID 23355237, compound

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

1.52 g from N-(2-chloroethyl)-7-chloro-4-quinolinamine hydrochloride; colourless crystals from acetonitrile, m.p.: 115°-117° C.

Sources & evidence

ORD record
ord-f727bbf8c5024bbb91bd26129ca9c59e
Source dataset
uspto-grants-1997_01
Patent number
US05596002

Reaction notes

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